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重金属对丝裂原活化蛋白激酶通路的影响。

Effects of heavy metals on mitogen-activated protein kinase pathways.

机构信息

Department of Environmental Toxicology, Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, 807-8555, Kitakyushu, Japan,

出版信息

Environ Health Prev Med. 2002 Jan;6(4):210-7. doi: 10.1007/BF02897972.

Abstract

The signaling pathways leading to cellular protection or cell death following exposure to heavy metals have not been fully clarified. Mitogen-activated protein kinases (MAPKs), i.e., extracellular signal-regulated protein kinase (ERK), c-Jun NH(2)-terminal kinase (JNK) and p38 MAPK transmit extracellular signals into the nucleus, and have been shown to participate in a diverse array of cellular functions such as cell growth, differentiation and apoptosis. Treatment with cadmium, inorganic mercury or tributyltin can activate ERK, JNK and p38 MAPK, and induces the expression of c-fos and c-jun genes prior to the development of apoptosis. However, the members of the MAPK family appear to be differentially activated depending on the heavy metal and the cell type exposed. Consequently, various cellular responses may be caused by the distinct pattern of MAPKs activation. MAPKs may be one of the important cellular signal transduction pathways affected by various environmental pollutants, including heavy metals.

摘要

重金属暴露后导致细胞保护或细胞死亡的信号通路尚未完全阐明。丝裂原活化蛋白激酶(MAPKs),即细胞外信号调节蛋白激酶(ERK)、c-Jun N 末端激酶(JNK)和 p38MAPK 将细胞外信号转导至细胞核,并已被证明参与多种细胞功能,如细胞生长、分化和凋亡。用镉、无机汞或三丁基锡处理可以激活 ERK、JNK 和 p38MAPK,并在细胞凋亡发生之前诱导 c-fos 和 c-jun 基因的表达。然而,MAPK 家族的成员似乎根据暴露的重金属和细胞类型而被不同地激活。因此,不同的 MAPKs 激活模式可能会导致各种细胞反应。MAPKs 可能是受各种环境污染物(包括重金属)影响的重要细胞信号转导途径之一。

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